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ZooKeys 208: 17-25 (20 | 2) A peer-rev iewed open-access journa I 


doi: 10.3897/zookeys.208.328 | RESEARCH ARTICLE #Zookey 


www.zookeys.o rg Launched to accelerate biodiversity research 


A new species and new records of Laelaspis Berlese 
(Acari, Laelapidae) from Iran 


Omid Joharchi't, Mahdi Jalaeian?*, Saeed Paktinat-Saeej*§, Azadeh Ghafarian*" 


| Department of Plant Protection, Yazd Branch, Islamic Azad University, Yazd, Iran 2. Agriculture & Natural Re- 
sources Research Center of Khorasan Razavi Province, Plant Protection Department, Mashhad, Iran 3 Department 
of Plant Protection, College of Agriculture, Ferdowsi University of Mashhad, Iran 4 Department of Entomology, 
Collage of Agriculture, Khorasgan Branch, Islamic Azad University, Isfahan, Iran 


T urn:lsid:zoobank. org:author:708542 1 B-EBD9-430F-ACI B-A520DC4F38DC 
* urn:lsid:zoobank. org:author:78D97837-6130-46C1-BLEB-3DD1/CFO98E4 
§ urn:lid:zoobank.org:author:F82EC1F7-249B-449A-962D-CF280F673DD2 

| urn:lsid:zoobank. org:author:6EB9449 1-13 EE-4326-8E9A-9299E472DBA3 


Corresponding author: Omid Joharchi (joharchi@iauyazd.ac.ir) 


Academic editor: Andre Bochkov | Received 24 April 2012 | Accepted 9 July 2012 | Published 17 July 2012 
urn:lsid:zoobank.org:pub:0F0A8627-2D 99-4B2C-8 DF0-F23F429FODIF 


Citation: Joharchi O, Jalaeian M, Paktinat-Saeej S, Ghafarian A (2012) A new species and new records of Laelaspis Berlese 
(Acari, Laelapidae) from Iran. ZooKeys 208: 17—25. doi: 10.3897/zookeys.208.3281 


Abstract 

This paper reports on three species of mites of the genus Lae/aspis in Iran — Laelaspis calidus Berlese from 
Pheidole pallidula, L. humeratus (Berlese) from Tetramorium caespitum and L. dariusi Joharchi & Jalaeian, 
sp. n. from soil. The new species is described and illustrations provided. 


Keywords 


Laelapidae, taxonomy, Formicidae, Iran, myrmecophiles 


Introduction 


The Laelapidae is one of the largest families of free-living Mesostigmata, but it has not 
yet achieved a stable classification (Tenorio 1982, Joharchi et al. in press). Hypoaspis 
Canestrini and related genera have had an especially complicated and confusing 
history, including Laelaspis Berlese, 1903, which has often been treated as a subgenus 


Copyright Omid Joharchi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License 3.0 
(CC-BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 


18 Omid Joharchi et al. / ZooKeys 208: 17-25 (2012) 


of Hypoaspis Canestrini, 1884 (Hunter 1961, Hunter and Glover 1968, Karg 1982, 
1993, Faraji et al. 2008). Joharchi et al. (2011) treated Laelaspis as a separate genus, 
and gave a diagnosis and comparison of diagnostic characters for the closely related 
genera Gymnolaelaps and Pseudoparasitus. That concept of Laelapsis is followed here. 

Joharchi et al. previously reported on five species of mites of the genus Laelaspis 
and on several genera associated with ants in Iran (Joharchi et al. in press, Joharchi et 
al. 2011). Joharchi et al. have previously provided a key to species of Laelaspis occur- 
ring in the Western Palaearctic Region with a summary of their host associations and 
biology (Joharchi et al. in press). We now expand the study to include further species 
in the genus Laelaspis Berlese, 1903, mainly associated with ants and soil. 

The cosmopolitan genus Laelaspis includes 17 species in the Western Palaearctic 
Region and most species are associated with ants or their nests. However, a few were 
collected with small mammals or in soil, and most species have only been collected on 
few occasions, so it is difficult to draw any firm conclusions about their host specificity 
(Joharchi et al. in press). Six species of Laelaspis have been reported previously from 
Iran (Joharchi et al. in press). Unidentified species of Laelaspis were also reported from 
Iran by Kamali et al. (2001) and Nemati and Babaeian (2010). The purpose of this 
paper is to describe another species of Lae/aspis and increase our knowledge of the 
Iranian fauna of Laelapidae. 


Materials and methods 


Mites associated with ants and soil were collected in Alborz, Khorasan, Kerman and 
Yazd Provinces over a period of two years (2010-2012). Mites were removed from 
ants’ nests by individual hand picking and by extraction from ant nest and soil mate- 
rial using Tullgren funnels. Mites were cleared in Nesbitt’s solution and mounted in 
Hoyer’s medium. The nomenclature used for the dorsal idiosomal chaetotaxy is that of 
Lindquist and Evans (1965), the leg chaetotaxy is that of Evans (1963a) the palp chae- 
totaxy that of Evans (1963b), and names of other anatomical structures mostly follow 
Evans and Till (1979). We use the term “lyrifissures” to refer to slit-shaped sensilli, 
and “pore” for circular or oval-shaped cuticular openings of unspecified function. The 
holotype and paratypes of the new species are deposited in the Acarological collection, 
Department of Plant Protection, Yazd Branch, Islamic Azad University (YIAU); para- 
types are also deposited in the Jalal Afshar Zoological Museum, College of Agriculture, 
University of Tehran, Iran (JAZM) and in the Australian National Insect Collection, 
CSIRO Ecosystem Sciences, Canberra, Australia (ANIC). All measurements in the 
descriptions are given in micrometres (um). 


A new species and new records of Laelaspis Berlese (Acari, Laelapidae) from Iran 19 


Results 


Genus Laelaspis Berlese 
http://species-id.net/wiki/Laelaspis 


Laelaps (Laelaspis) Berlese, 1903: 13. 


Type species. Laelaps astronomicus Koch, 1839, by original designation. 

Diagnosis. See Joharchi et al. (2011). 

Notes on the genus. Laelaspis belongs to a group of genera of Laelapidae in 
which the genital shield of the female is greatly expanded, so that its posterior 
margin abuts the anal shield and its lateral margins extend outward behind coxae 
IV. The expanded genito-ventral shield in these genera captures at least two pairs of 
ventral setae in addition to the genital setae on the the extreme edges of the shield. 
Laelaspis is distinguished from Gymnolaelaps by its two-tined palp tarsal claw, the 
absence of pre-sternal shields, and the presence of two distinct A-shaped lines on 
the genital shield. Laelaspis differs from Pseudoparasitus because Pseudoparasitus has 
at least two pairs of setae on the surface of the genital shield, well separated from 
the edges of the shield, while all the genital setae of Laelaspis and Gymnolaelaps are 
on the extreme edges of the shield. 


Laelaspis calidus Berlese 
http://species-id.net/wiki/Laelaspis_calidus 


Laelaspis calidus Berlese, 1924: 255; Hunter 1961: 676. 
Hypoaspis (Laelaspis) calidus— Aswegen and Loots 1970: 27. 
Hypoaspis (Laelaspis) calida— Karg 1982: 250; 1989: 120. 


Specimens examined. Six females, Anar, Kerman, 53°30'N, 18°55’E, alt. 1152 m 10 
November 2011, O. Joharchi coll., in nest of Pheidole pallidula. 

Notes. Laelaspis calidus was described from east Africa (Berlese 1924), also has 
been recorded at Kilimanjaro near Marangu from moss and litter (Aswegen and Loots 
1970) and has not been reported since. It is easily recognised by the bidentate movable 
digit and the seven-toothed fixed digit, the serrated postanal seta and seta Z5 two to 
three times as long as J5. This species has been found from moss and litter, but has not 
been reported from the nests of ants. It is now recorded in Iran for the first time from 
the ant nests. 


20 Omid Joharchi et al. / ZooKeys 208: 17-25 (2012) 


Laelaspis dariusi Joharchi & Jalaeian sp. n. 
urn:lsid:zoobank.org:act:BB2DA9B6-4ACF-4F3B-A5 16-3E33EA3AD1F0 
http://species-id.net/wiki/Laelaspis_dariusi 

Figures 1-8 


Specimens examined. Holotype, female, Iran, Khorasan Razavi Province, Kalate Na- 
deri (Laeen), 37°07'N, 59°29'E, alt. 858 m, 26 Mar 2010, S. Paktinat-saeej coll., in 
soil of apple orchard. Paratypes, seven females, same data as holotype (in YIAU, JAZM 
and ANIC). 

Description of the female. Figures 1-8. Dorsal idiosoma. Dorsal shield length 
524-534, width 406-426 (n = 8) (Fig. 1). Shield oval shaped, with reticulation, more 
distinct in opisthonotal region; with 39 pairs of long setae, 22 podonotal, 17 opistho- 
notal, including two pairs of Zx setae between J and Z setae, almost all setae slightly 
swollen at base, with pointed tip (Fig. 4), podonotal setae very long, reaching well 
past base of next posterior setae, setae of central area of dorsal shield decreasing in 
length from anterior to posterior (j3, z2 74-82, j4 69-74, j6, J1, J3 54-57), lateral setae 
thicker than central setae, almost all marginal setae including Z5 slightly serrated (Fig. 
3), length 89-99, almost double length of J5, length 45—50; opisthonotal region with 
three unpaired supernumerary seta Jx in each specimen. Shield with three pairs of large 
circular to oval-shaped pores, other pores inconspicuous. 

Ventral idiosoma (Fig. 2). Tritosternum with columnar base (15-17 long x 9-10 
wide), paired pilose laciniae, length 67—69 (Fig. 7), pre-sternal shields absent, pre- 
sternal area with some weak transverse lines. Sternal shield length 111-116, narrow- 
est between coxae II (87-89) widest between coxae II & II (151-153), with slightly 
concave posterior margin and undulating anterior margin, with three pairs of long 
and smooth sternal setae, stl 42—47, st2 59-62, st3 67-69, reaching well past base 
of next posterior setae, one pair of lyrifissures adjacent to setae stl, a pair of larger 
lyrifissures between st2 and s¢3; antero-lateral surface of sternal shield with line- 
ate ornamentation, central area smooth. Metasternal platelets absent, metasternal 
setae st4 (27-32) and metasternal pores located in soft skin; endopodal plates II/III 
fused to sternal shield, endopodal plates IH/IV elongate, narrow, curved. Genital 
shield broad, length 277-285, maximum width 248-260, posterior margin round- 
ed, abutting anal shield, surface with characteristic ornamentation including dis- 
tinct A-shaped lines and polygonal ornamentation, bearing the long genital setae st5 
(87-89) and two pairs of long setae (89-99) on its lateral edges. Paragenital pores 
located on soft skin lateral to shield behind coxae IV. Anal shield subtriangular, 
length 104-109, width 126-131; its anterior half with lineate ornamentation and a 
pair of lateral pores; post-anal seta 42-45 um, longer and thicker than para-anal se- 
tae, 22—25. Opisthogastric skin with long, narrow and oval metapodal plates (62—64 
long x 8-10 wide) very close to genital shield, and 15 pairs of slightly serrate setae, 
each arising on small sclerotised platelet, and seven pairs of pores. Exopodal plates 
forming subtriangular extensions behind coxae IV, narrow elongate exopodal plates 
I/II not fused to peritrematal shield. Peritreme extending from coxa IV to anterior 


A new species and new records of Laelaspis Berlese (Acari, Laelapidae) from Iran ZA 


l 2 


50 um 


Figures |-8. Laelaspis dariusi Joharchi and Jalaeian sp. n., female. | Dorsal shield 2 Ventral idiosoma 
3 Seta Z5 enlarged 4 Dorsal shield seta s3 5 Hypostome 6 Epistome 7 Tritosternum 8 Chelicera. 


22 Omid Joharchi et al. / ZooKeys 208: 17-25 (2012) 


of coxa I, peritrematal shield narrow, post-stigmatal section conspicuous, with two 
pairs of pores. 

Gnathosoma. Epistome triangular, smooth (Fig. 6). Hypostomal groove with six 
rows of denticles each bearing 8—10 small teeth, and smooth anterior transverse line. 
Hypostome with four pairs of setae, internal posterior hypostomal setae h3 longest 
(Fig. 5). Corniculi robust and horn-like, reaching mid-level of palp femur. Palp chae- 
totaxy: trochanter 2 (v1 thick), femur 5, genu 6, tibia 12, tarsus 15; all setae smooth 
and needle-like, palp tarsal claw two-tined. Fixed digit of chelicera with six blunt teeth 
(Fig. 8); pilus dentilis short and robust; dorsal seta short, prostrate; movable digit with 
two teeth; arthrodial membrane with a rounded flap and short filaments. 

Legs. Legs I and III short (302-312, 282-288), I and IV longer (430-446, 372- 
392). Leg I: coxa 0 0/1 0/1 0, trochanter 1 1/1 0/2 1 (ad thick), femur 2 3/2 2/2 2 
(ad2, ad3, all, pl1 and p/2 thick), genu 2 3/2 3/1 2 (all dorsal thick), tibia 2 3/2 3/1 
2. Leg II: coxa 0 0/1 0/1 0 (all setae thick), trochanter 1 0/1 1/2 1, femur 2 3/1 2/2 
1 (ad1, pd2 and pv1 thick), genu 2 3/1 2/1 2 (all ventral thick), tibia 2 2/1 2/1 2 (all 
ventral thick). Leg HI: coxa 0 0/1 0/1 0 (all setae thick), trochanter 1 0/1 0/2 1 (al 
and av thick), femur 1 2/1 1/0 1 (adI and ad2 thick), genu 2 2/1 2/1 1 (ventral setae 
thick), tibia: 2 1/1 2/1 1(ventral setae thick). Leg IV: coxa 0 0/1 0/0 0, trochanter 1 
0/1 0/2 1 (av thick), femur 1 2/1 1/0 1 (a/long, ad1 and ad2 thick), genu 2 2/1 3/0 1 
(ventral thick), tibia 2 1/1 3/1 2; all setae fine and needle-like unless otherwise noted. 
Tarsi I-I[V with 18 setae 3 3/2 3/2 3 + mv, md. All pre-tarsi with a pair of claws and a 
long thin membranous ambulacrum. 

Insemination structures not seen, apparently unsclerotised. 

Etymology. The species is named in memory of Darius I (Old Persian: Darayava(h)us), 
also known as Darius the Great, was the third king of the Achaemenid Empire, who proved 
to be a strong and wise ruler and he was tolerant toward other religions and cultures, pro- 
moted learning, agriculture, forestation, and the construction of highways. He also built 
the great palace cities of Susa and Persepolis. 

Notes. Laelaspis dariusi differs from all other species in the genus by its dorsal 
shield setae in central area decreasing in length from anterior to posterior, seta Z5 much 
longer than J5; seta vl on the palp trochanter thick, sternal setae long and smooth, 
long enough to well past base of next posterior setae, movable digit of chelicera with 
two teeth and fixed digit of chelicera with six blunt teeth. 


Laelaspis humeratus (Berlese) 
http://species-id.net/wiki/Laelaspis_humeratus 


Laelaps (Laelaspis) humeratus Berlese 1904: 425. 

Hypoaspis humerata.— Evans and Till 1966: 212; Lapina 1976: 43. 

Laelaspis humeratus— Hull 1925: 210; Willmann 1951:113; Hunter 1961: 675; 
Salmane 2001a: 131; Salmane 2001b: 34; Salmane and Brumelis 2010: 390. 

Hypoaspis (Laelaspis) humerata.— Karg 1979: 102; 1982: 250; 1989: 120. 


A new species and new records of Laelaspis Berlese (Acari, Laelapidae) from Iran 23 


Laelaspis humerata.— Bregetova 1977: 545. 


Specimens examined. One female, Alborz, Karaj, 35°56'N, 51°22’E, alt. 2000 m, 11 
July 2011, O. Joharchi coll., in nest of Zetramorium caespitum. 

Notes. Laelaspis humeratus was described from Luxemburg (Berlese 1904), and 
has been recorded from Latvia (Lapina 1976; Salmane 2001a, 2001b), Russia and 
Austria (Bregetova 1977), and England (Hull 1925; Evans and Till 1966). This species 
was found associated with at least two genera of ants (Lasius and Tetramorium), free- 
living in soil, litter and meadows, and from the nests of mammals. This species is 
easily recognised by the large number of long, thick and wavy opisthonotal setae, 
the bidentate movable digit and the tridentate fixed digit. Haddad Irani-Nejad et al. 
(2003) recorded an unidentified species as Laelaspis near humerata (Berlese, 1904), but 
the identity of that species cannot be confirmed because the specimens have been lost, 
so this is the first record of L. humeratus from Iran. 


Discussion 


Before the start of this study, six species of Laelaspis had been reported from Iran. We 
have added new information on L. calidus and L. humeratus. 

Joharchi et al. have previously discussed the distinction between Laelaspis and 
Gymnolaelaps and Pseudoparasitus (Joharchi et al. 2011). The biology of most species of 
Laelaspis has not been studied, but the limited information that is available shows that 
they are predatory (Hunter 1964). Laelaspis appears to be a genus of predators that feed 
on other small invertebrates in their hosts’ nests, but are not harmful to the ants. High 
populations of acarids may be harmful to ants, so the presence of predators such as Laelaspis 
may be beneficial, forming a symbiotic relationship with its ant hosts. The ecological role 
of Laelaspis in mammal nests is also unknown, but it appears likely that they are predators, 
feeding on other nest inhabitants such as acarid mites (Rasmy et al. 1987). 


Acknowledgements 


We are indebted to Dr. Bruce Halliday (CSIRO Entomology, Canberra, Australia) 
for his all helpful and valuable comments. This study was supported by Yazd branch, 
Islamic Azad University, Yazd, Iran wich is greatly appreciated. We are very grateful to 
the reviewers for their comments. 


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